Britannica AI Icon

Quick Summary

Monosomy is a genetic condition where an individual has one less chromosome than the typical diploid number. In humans, this means having 45 chromosomes instead of the usual 46. This occurs due to errors in cell division, specifically during meiosis, leading to an egg or sperm cell with a missing chromosome.123

While trisomy, the presence of an extra chromosome, can result in conditions like Down syndrome, monosomy of autosomes is typically lethal in utero and not observed in live births. Monosomy is a type of chromosomal disorder, which arises from abnormal chromosome number or structure.24

Summary created from Britannica articles using AI. AI can make mistakes, so verify using Britannica articles.

Ask Britannica AI about this topic

Britannica doesn't have a full article on this topic, so we've curated a list of our relevant coverage.